Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g00280 | A07 | 127903 | C | T | missense_variant | MODERATE | c.281G>A|p.Gly94Glu |
S138 |
2 | BAA07g00280 | A07 | 127916 | G | A | synonymous_variant | LOW | c.268C>T|p.Leu90Leu |
S266 |
3 | BAA07g00280 | A07 | 128302 | C | T | missense_variant | MODERATE | c.61G>A|p.Asp21Asn |
S130 |
4 | BAA07g00280 | A07 | 133028 | G | A | upstream_gene_variant | MODIFIER | c.-4666C>T| |
S65 |
5 | BAA07g00280 | A07 | 133138 | C | T | upstream_gene_variant | MODIFIER | c.-4776G>A| |
S260 |
6 | BAA07g00280 | A07 | 133219 | C | T | upstream_gene_variant | MODIFIER | c.-4857G>A| |
S205 |